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Sequential proton transfer through water bridges in acid-base reactions.

Science (New York, N.Y.)

Mohammed OF, Pines D, Dreyer J, Pines E, Nibbering ET.
PMID: 16210532
Science. 2005 Oct 07;310(5745):83-6. doi: 10.1126/science.1117756.

The proton transfer mechanism between aqueous Brønsted acids and bases, forming an encounter pair, has been studied in real time with ultrafast infrared spectroscopy. The transient intermediacy of a hydrated proton, formed by ultrafast dissociation from an optically triggered...

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Mohammed OF, Pines D, Dreyer J, et al. Sequential proton transfer through water bridges in acid-base reactions. Science. 2005;310(5745):83-6doi: 10.1126/science.1117756.
Mohammed, O. F., Pines, D., Dreyer, J., Pines, E., & Nibbering, E. T. (2005). Sequential proton transfer through water bridges in acid-base reactions. Science (New York, N.Y.), 310(5745), 83-6. https://doi.org/10.1126/science.1117756
Mohammed, Omar F, et al. "Sequential proton transfer through water bridges in acid-base reactions." Science (New York, N.Y.) vol. 310,5745 (2005): 83-6. doi: https://doi.org/10.1126/science.1117756
Mohammed OF, Pines D, Dreyer J, Pines E, Nibbering ET. Sequential proton transfer through water bridges in acid-base reactions. Science. 2005 Oct 07;310(5745):83-6. doi: 10.1126/science.1117756. PMID: 16210532.
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Generation of femtosecond Bessel beams with microaxicon arrays.

Optics letters

Grunwald R, Griebner U, Tschirschwitz F, Nibbering ET, Elsaesser T, Kebbel V, Hartmann HJ, Jüptner W.
PMID: 18064247
Opt Lett. 2000 Jul 01;25(13):981-3. doi: 10.1364/ol.25.000981.

Multiple quasi-Bessel beams are generated by transmission of sub-30-fs pulses from a Ti:sapphire laser through refractive thin-film microaxicon arrays. Time-integrated intensity distributions at several axial positions and for pulse durations of 26 and 12.5 fs reveal significant changes of...

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Grunwald R, Griebner U, Tschirschwitz F, et al. Generation of femtosecond Bessel beams with microaxicon arrays. Opt Lett. 2000;25(13):981-3doi: 10.1364/ol.25.000981.
Grunwald, R., Griebner, U., Tschirschwitz, F., Nibbering, E. T., Elsaesser, T., Kebbel, V., Hartmann, H. J., & Jüptner, W. (2000). Generation of femtosecond Bessel beams with microaxicon arrays. Optics letters, 25(13), 981-3. https://doi.org/10.1364/ol.25.000981
Grunwald, R, et al. "Generation of femtosecond Bessel beams with microaxicon arrays." Optics letters vol. 25,13 (2000): 981-3. doi: https://doi.org/10.1364/ol.25.000981
Grunwald R, Griebner U, Tschirschwitz F, Nibbering ET, Elsaesser T, Kebbel V, Hartmann HJ, Jüptner W. Generation of femtosecond Bessel beams with microaxicon arrays. Opt Lett. 2000 Jul 01;25(13):981-3. doi: 10.1364/ol.25.000981. PMID: 18064247.
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Ultrafast branching of reaction pathways in 2-(2'-hydroxyphenyl)benzothiazole in polar acetonitrile solution.

The journal of physical chemistry. A

Mohammed OF, Luber S, Batista VS, Nibbering ET.
PMID: 21604716
J Phys Chem A. 2011 Jul 07;115(26):7550-8. doi: 10.1021/jp202277t. Epub 2011 Jun 09.

In a combined study on the photophysics of 2-(2'-hydroxyphenyl)-benzothiazole (HBT) in polar acetonitrile utilizing ultrafast infrared spectroscopy and quantum chemical calculations, we show that a branching of reaction pathways occurs on femtosecond time scales. Apart from the excited-state intramolecular...

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Mohammed OF, Luber S, Batista VS, et al. Ultrafast branching of reaction pathways in 2-(2'-hydroxyphenyl)benzothiazole in polar acetonitrile solution. J Phys Chem A. 2011;115(26):7550-8doi: 10.1021/jp202277t.
Mohammed, O. F., Luber, S., Batista, V. S., & Nibbering, E. T. (2011). Ultrafast branching of reaction pathways in 2-(2'-hydroxyphenyl)benzothiazole in polar acetonitrile solution. The journal of physical chemistry. A, 115(26), 7550-8. https://doi.org/10.1021/jp202277t
Mohammed, Omar F, et al. "Ultrafast branching of reaction pathways in 2-(2'-hydroxyphenyl)benzothiazole in polar acetonitrile solution." The journal of physical chemistry. A vol. 115,26 (2011): 7550-8. doi: https://doi.org/10.1021/jp202277t
Mohammed OF, Luber S, Batista VS, Nibbering ET. Ultrafast branching of reaction pathways in 2-(2'-hydroxyphenyl)benzothiazole in polar acetonitrile solution. J Phys Chem A. 2011 Jul 07;115(26):7550-8. doi: 10.1021/jp202277t. Epub 2011 Jun 09. PMID: 21604716.
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Ultrafast nonlinear spectroscopy with chirped optical pulses.

Physical review letters

Duppen K, Nibbering ET, Wiersma DA.
PMID: 10045916
Phys Rev Lett. 1992 Jan 27;68(4):514-517. doi: 10.1103/PhysRevLett.68.514.

No abstract available.

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Duppen K, Nibbering ET, Wiersma DA. Ultrafast nonlinear spectroscopy with chirped optical pulses. Phys Rev Lett. 1992;68(4):514-517doi: 10.1103/PhysRevLett.68.514.
Duppen, K., Nibbering, E. T., & Wiersma, D. A. (1992). Ultrafast nonlinear spectroscopy with chirped optical pulses. Physical review letters, 68(4), 514-517. https://doi.org/10.1103/PhysRevLett.68.514
Duppen, et al. "Ultrafast nonlinear spectroscopy with chirped optical pulses." Physical review letters vol. 68,4 (1992): 514-517. doi: https://doi.org/10.1103/PhysRevLett.68.514
Duppen K, Nibbering ET, Wiersma DA. Ultrafast nonlinear spectroscopy with chirped optical pulses. Phys Rev Lett. 1992 Jan 27;68(4):514-517. doi: 10.1103/PhysRevLett.68.514. PMID: 10045916.
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Gas phase bimolecular chemistry of isomeric C3H 6Br (+) cations.

Journal of the American Society for Mass Spectrometry

Heck AJ, Nibbering NM.
PMID: 24222056
J Am Soc Mass Spectrom. 1995 Jan;6(1):11-8. doi: 10.1016/1044-0305(94)00084-D.

The gas phase chemistry of C3H6Br(+) cations generated via low energy electron impact on various dibromopropanes has been studied by using Fourier transform ion cyclotron resonance mass spectrometry. Neutral substrate molecules that have been selected to probe the bimolecular...

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Heck AJ, Nibbering NM. Gas phase bimolecular chemistry of isomeric C3H 6Br (+) cations. J Am Soc Mass Spectrom. 1995;6(1):11-8doi: 10.1016/1044-0305(94)00084-D.
Heck, A. J., & Nibbering, N. M. (1995). Gas phase bimolecular chemistry of isomeric C3H 6Br (+) cations. Journal of the American Society for Mass Spectrometry, 6(1), 11-8. https://doi.org/10.1016/1044-0305(94)00084-D
Heck, A J, and Nibbering, N M. "Gas phase bimolecular chemistry of isomeric C3H 6Br (+) cations." Journal of the American Society for Mass Spectrometry vol. 6,1 (1995): 11-8. doi: https://doi.org/10.1016/1044-0305(94)00084-D
Heck AJ, Nibbering NM. Gas phase bimolecular chemistry of isomeric C3H 6Br (+) cations. J Am Soc Mass Spectrom. 1995 Jan;6(1):11-8. doi: 10.1016/1044-0305(94)00084-D. PMID: 24222056.
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Chemical ionization of phenyl n-propyl ether and methyl substituted analogs: Propene loss initiated by competing proton transfer to the oxygen atom and the aromatic ring.

Journal of the American Society for Mass Spectrometry

Bogdanov B, Matimba HE, Ingemann S, Nibbering NM.
PMID: 24203479
J Am Soc Mass Spectrom. 1996 Jul;7(7):639-52. doi: 10.1016/1044-0305(96)00002-5.

The mechanism of propene loss from protonated phenyl n-propyl ether and a series of mono-, di-, and trimethylphenyl n-propyl ethers has been examined by chemical ionization (CI) mass spectrometry in combination with tandem mass spectrometry experiments. The role of...

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Bogdanov B, Matimba HE, Ingemann S, et al. Chemical ionization of phenyl n-propyl ether and methyl substituted analogs: Propene loss initiated by competing proton transfer to the oxygen atom and the aromatic ring. J Am Soc Mass Spectrom. 1996;7(7):639-52doi: 10.1016/1044-0305(96)00002-5.
Bogdanov, B., Matimba, H. E., Ingemann, S., & Nibbering, N. M. (1996). Chemical ionization of phenyl n-propyl ether and methyl substituted analogs: Propene loss initiated by competing proton transfer to the oxygen atom and the aromatic ring. Journal of the American Society for Mass Spectrometry, 7(7), 639-52. https://doi.org/10.1016/1044-0305(96)00002-5
Bogdanov, B, et al. "Chemical ionization of phenyl n-propyl ether and methyl substituted analogs: Propene loss initiated by competing proton transfer to the oxygen atom and the aromatic ring." Journal of the American Society for Mass Spectrometry vol. 7,7 (1996): 639-52. doi: https://doi.org/10.1016/1044-0305(96)00002-5
Bogdanov B, Matimba HE, Ingemann S, Nibbering NM. Chemical ionization of phenyl n-propyl ether and methyl substituted analogs: Propene loss initiated by competing proton transfer to the oxygen atom and the aromatic ring. J Am Soc Mass Spectrom. 1996 Jul;7(7):639-52. doi: 10.1016/1044-0305(96)00002-5. PMID: 24203479.
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Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling.

The journal of physical chemistry. A

Mohammed OF, Xiao D, Batista VS, Nibbering ET.
PMID: 24684387
J Phys Chem A. 2014 May 01;118(17):3090-9. doi: 10.1021/jp501612f. Epub 2014 Apr 17.

We combine ultrafast electronic and vibrational spectroscopy and computational modeling to investigate the photoinduced excited-state intramolecular hydrogen-transfer dynamics in 1,8-dihydroxy-9,10-anthraquinone (DHAQ) in tetrachloroethene, acetonitrile, dimethyl sulfoxide, and methanol. We analyze the electronic excited states of DHAQ with various possible...

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Mohammed OF, Xiao D, Batista VS, et al. Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling. J Phys Chem A. 2014;118(17):3090-9doi: 10.1021/jp501612f.
Mohammed, O. F., Xiao, D., Batista, V. S., & Nibbering, E. T. (2014). Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling. The journal of physical chemistry. A, 118(17), 3090-9. https://doi.org/10.1021/jp501612f
Mohammed, Omar F, et al. "Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling." The journal of physical chemistry. A vol. 118,17 (2014): 3090-9. doi: https://doi.org/10.1021/jp501612f
Mohammed OF, Xiao D, Batista VS, Nibbering ET. Excited-state intramolecular hydrogen transfer (ESIHT) of 1,8-dihydroxy-9,10-anthraquinone (DHAQ) characterized by ultrafast electronic and vibrational spectroscopy and computational modeling. J Phys Chem A. 2014 May 01;118(17):3090-9. doi: 10.1021/jp501612f. Epub 2014 Apr 17. PMID: 24684387.
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Antimicrobial Peptides in Biomedical Device Manufacturing.

Frontiers in chemistry

Riool M, de Breij A, Drijfhout JW, Nibbering PH, Zaat SAJ.
PMID: 28971093
Front Chem. 2017 Aug 24;5:63. doi: 10.3389/fchem.2017.00063. eCollection 2017.

Over the past decades the use of medical devices, such as catheters, artificial heart valves, prosthetic joints, and other implants, has grown significantly. Despite continuous improvements in device design, surgical procedures, and wound care, biomaterial-associated infections (BAI) are still...

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Riool M, de Breij A, Drijfhout JW, et al. Antimicrobial Peptides in Biomedical Device Manufacturing. Front Chem. 2017;5:63doi: 10.3389/fchem.2017.00063.
Riool, M., de Breij, A., Drijfhout, J. W., Nibbering, P. H., & Zaat, S. A. J. (2017). Antimicrobial Peptides in Biomedical Device Manufacturing. Frontiers in chemistry, 563. https://doi.org/10.3389/fchem.2017.00063
Riool, Martijn, et al. "Antimicrobial Peptides in Biomedical Device Manufacturing." Frontiers in chemistry vol. 5 (2017): 63. doi: https://doi.org/10.3389/fchem.2017.00063
Riool M, de Breij A, Drijfhout JW, Nibbering PH, Zaat SAJ. Antimicrobial Peptides in Biomedical Device Manufacturing. Front Chem. 2017 Aug 24;5:63. doi: 10.3389/fchem.2017.00063. eCollection 2017. PMID: 28971093; PMCID: PMC5609632.
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SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection.

Frontiers in microbiology

Scheper H, Wubbolts JM, Verhagen JAM, de Visser AW, van der Wal RJP, Visser LG, de Boer MGJ, Nibbering PH.
PMID: 33584628
Front Microbiol. 2021 Jan 29;12:625952. doi: 10.3389/fmicb.2021.625952. eCollection 2021.

Prosthetic joint infection (PJI) is a severe complication of arthroplasty. Due to biofilm and persister formation current treatment strategies often fail. Therefore, innovative anti-biofilm and anti-persister agents are urgently needed. Antimicrobial peptides with their broad antibacterial activities may be...

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Scheper H, Wubbolts JM, Verhagen JAM, et al. SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection. Front Microbiol. 2021;12:625952doi: 10.3389/fmicb.2021.625952.
Scheper, H., Wubbolts, J. M., Verhagen, J. A. M., de Visser, A. W., van der Wal, R. J. P., Visser, L. G., de Boer, M. G. J., & Nibbering, P. H. (2021). SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection. Frontiers in microbiology, 12625952. https://doi.org/10.3389/fmicb.2021.625952
Scheper, Henk, et al. "SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection." Frontiers in microbiology vol. 12 (2021): 625952. doi: https://doi.org/10.3389/fmicb.2021.625952
Scheper H, Wubbolts JM, Verhagen JAM, de Visser AW, van der Wal RJP, Visser LG, de Boer MGJ, Nibbering PH. SAAP-148 Eradicates MRSA Persisters Within Mature Biofilm Models Simulating Prosthetic Joint Infection. Front Microbiol. 2021 Jan 29;12:625952. doi: 10.3389/fmicb.2021.625952. eCollection 2021. PMID: 33584628; PMCID: PMC7879538.
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The Spatio-Temporal Distribution of Cell Wall-Associated Glycoproteins During Wood Formation in .

Frontiers in plant science

Abedi T, Castilleux R, Nibbering P, Niittylä T.
PMID: 33381142
Front Plant Sci. 2020 Dec 15;11:611607. doi: 10.3389/fpls.2020.611607. eCollection 2020.

Plant cell wall associated hydroxyproline-rich glycoproteins (HRGPs) are involved in several aspects of plant growth and development, including wood formation in trees. HRGPs such as arabinogalactan-proteins (AGPs), extensins (EXTs), and proline rich proteins (PRPs) are important for the development...

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Abedi T, Castilleux R, Nibbering P, et al. The Spatio-Temporal Distribution of Cell Wall-Associated Glycoproteins During Wood Formation in . Front Plant Sci. 2020;11:611607doi: 10.3389/fpls.2020.611607.
Abedi, T., Castilleux, R., Nibbering, P., & Niittylä, T. (2020). The Spatio-Temporal Distribution of Cell Wall-Associated Glycoproteins During Wood Formation in . Frontiers in plant science, 11611607. https://doi.org/10.3389/fpls.2020.611607
Abedi, Tayebeh, et al. "The Spatio-Temporal Distribution of Cell Wall-Associated Glycoproteins During Wood Formation in ." Frontiers in plant science vol. 11 (2020): 611607. doi: https://doi.org/10.3389/fpls.2020.611607
Abedi T, Castilleux R, Nibbering P, Niittylä T. The Spatio-Temporal Distribution of Cell Wall-Associated Glycoproteins During Wood Formation in . Front Plant Sci. 2020 Dec 15;11:611607. doi: 10.3389/fpls.2020.611607. eCollection 2020. PMID: 33381142; PMCID: PMC7768015.
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A computational study of the double hydrogen migration in the molecular ions of endo tricyclo[5.2.1.0(2,6)]decene.

Journal of the American Society for Mass Spectrometry

Nibbering NM, van der Hart WJ.
PMID: 12387324
J Am Soc Mass Spectrom. 2002 Oct;13(10):1186-9. doi: 10.1016/S1044-0305(02)00449-X.

Previous field ionization kinetic experiments have supported strongly that the double hydrogen migration prior to the elimination of C5H8 from the molecular ions of the endo isomers of 8,9-disubstituted tricyclo[5.2.1.0(2,6)]decenes, which is not observed for the exo isomers, proceeds...

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Nibbering NM, van der Hart WJ. A computational study of the double hydrogen migration in the molecular ions of endo tricyclo[5.2.1.0(2,6)]decene. J Am Soc Mass Spectrom. 2002;13(10):1186-9doi: 10.1016/S1044-0305(02)00449-X.
Nibbering, N. M., & van der Hart, W. J. (2002). A computational study of the double hydrogen migration in the molecular ions of endo tricyclo[5.2.1.0(2,6)]decene. Journal of the American Society for Mass Spectrometry, 13(10), 1186-9. https://doi.org/10.1016/S1044-0305(02)00449-X
Nibbering, Nico M M, and van der Hart, Wim J. "A computational study of the double hydrogen migration in the molecular ions of endo tricyclo[5.2.1.0(2,6)]decene." Journal of the American Society for Mass Spectrometry vol. 13,10 (2002): 1186-9. doi: https://doi.org/10.1016/S1044-0305(02)00449-X
Nibbering NM, van der Hart WJ. A computational study of the double hydrogen migration in the molecular ions of endo tricyclo[5.2.1.0(2,6)]decene. J Am Soc Mass Spectrom. 2002 Oct;13(10):1186-9. doi: 10.1016/S1044-0305(02)00449-X. PMID: 12387324.
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Host Immune Responses to .

Frontiers in microbiology

Nibbering B, Gerding DN, Kuijper EJ, Zwittink RD, Smits WK.
PMID: 34992590
Front Microbiol. 2021 Dec 21;12:804949. doi: 10.3389/fmicb.2021.804949. eCollection 2021.

No abstract available.

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Nibbering B, Gerding DN, Kuijper EJ, et al. Host Immune Responses to . Front Microbiol. 2021;12:804949doi: 10.3389/fmicb.2021.804949.
Nibbering, B., Gerding, D. N., Kuijper, E. J., Zwittink, R. D., & Smits, W. K. (2021). Host Immune Responses to . Frontiers in microbiology, 12804949. https://doi.org/10.3389/fmicb.2021.804949
Nibbering, Britt, et al. "Host Immune Responses to ." Frontiers in microbiology vol. 12 (2021): 804949. doi: https://doi.org/10.3389/fmicb.2021.804949
Nibbering B, Gerding DN, Kuijper EJ, Zwittink RD, Smits WK. Host Immune Responses to . Front Microbiol. 2021 Dec 21;12:804949. doi: 10.3389/fmicb.2021.804949. eCollection 2021. PMID: 34992590; PMCID: PMC8724541.
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Showing 25 to 36 of 78 entries